These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
456 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Ultra Violette recalled 44,497 tubes of its Mini SPF Mates kit on August 22, 2025. The sunscreen products showed inconsistent SPF results, including readings as low as SPF 4. Consumers must stop use immediately and contact the distributor for guidance.
Abbott Point Of Care recalled 6,115,950 i-STAT EG7+ cartridges on August 21, 2025. The recall stems from a lack of 510(k) premarket clearance for updated measurement ranges. This issue affects the accuracy of potassium and ionized calcium tests, posing a high risk to patients.
Latitude 36 Foods recalled 46,800 units of Honey Balsamic dressing on August 21, 2025. The dressing contains undeclared soy and sesame, posing a serious health risk. Consumers should not consume the product and seek a refund.
Folsom Metal Products recalled 10,960 units of 14 mm Distraction Pins on August 21, 2025. The recall follows concerns that the labeling included an unvalidated shelf life. Healthcare providers and patients must stop using the device immediately.
Abbott Point Of Care recalled 8,962,450 i-STAT CG8+ cartridges on August 21, 2025. The recall affects cartridges lacking proper 510(k) premarket clearance for updated sample types. Patients and healthcare providers must stop using these devices immediately.
Abbott Point Of Care recalled 547,250 i-STAT EG6+ cartridges on August 21, 2025. The recall stems from a lack of 510(k) premarket clearance for updated sample types and measurement ranges. Healthcare providers and patients must stop using these cartridges immediately.
Folsom Metal Products recalled 3,790 distraction pins on August 21, 2025. The recall affects all lots distributed from August 1, 2020, to July 30, 2025. The labeling lacks a validated shelf life, posing a high hazard risk.
Folsom Metal Products recalled 2,700 units of distraction pins on August 21, 2025. The recall affects devices with unvalidated shelf life labeling. Patients and healthcare providers must stop using the product immediately.
Taylor Farms recalled 8,284 units of its Honey Balsamic Salad Kit on August 21, 2025. The recall stems from undeclared allergens including sesame and soy. Consumers should not consume the affected products and seek refunds or replacements.
Abbott Point Of Care recalled 9,067,050 i-STAT CG4+ cartridges on August 21, 2025. The recall stems from a lack of 510(k) premarket clearance reflecting updated sample types and measurement ranges. Healthcare providers must stop using the device immediately and follow recall instructions.
Folsom Metal Products recalled 490 units of its 16 mm distraction pin on August 21, 2025. The recall affects devices with unvalidated shelf life labeling. Patients and healthcare providers must stop using the device immediately.
IBC Technologies recalled CX Combi Boilers on August 21, 2025, due to a burn hazard. The defective models can exceed safe hot water temperatures. Consumers should stop using the affected units immediately.
Folsom Metal Products recalled 160 units of distraction pins due to unvalidated shelf life labeling. The recall affects devices distributed across multiple states, including California and Texas. Patients and healthcare providers should stop using the product immediately.
Folsom Metal Products recalled 10 double packs of 14 mm Distraction Pins on August 21, 2025. The recall affects devices with unvalidated shelf life labeling. Healthcare providers and patients must stop using these devices immediately.
Jessie's Lemon Meringue Pie is recalled due to undeclared Yellow#5. The recall affects over 136,000 units distributed across 13 states. Consumers should not consume the product and seek refunds.
Hostess recalled 60,630 cases of Ding Dongs on August 20, 2025, following reports of mold contamination. The recall affects various packaging sizes sold across multiple states. Consumers should not consume the product and seek refunds or replacements immediately.
Itacate Foods recalled 566 packages of CHARGE-UP CHILAQUILES on August 20, 2025. The product contains undeclared Yellow #5 and Yellow #6, posing a health risk. Consumers should not consume the product and seek a refund or replacement.
Itacate Foods recalled 154 packages of CAMPSITE LENTEJAS lentil soup on August 20, 2025. The recall follows the discovery of undeclared Yellow #5 and Yellow #6, which can cause allergic reactions. Consumers should stop using the product immediately.
Abiomed recalled 71 Automated Impella Controllers on August 20, 2025. The devices may fail to perform correctly, leading to pump stoppage. Healthcare providers and patients must stop using these devices immediately.
Baxter Healthcare Corporation recalled 13,000 containers of Acetaminophen Injection on August 20, 2025. The recall follows reports of discoloration that may affect product safety. Consumers should stop using the medication immediately and contact their healthcare providers for guidance.